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What is Night blindness, congenital stationary, type 2A?

What is Night blindness, congenital stationary, type 2A?

  • Night blindness, congenital stationary, type 2A: A rare X-linked disorder of the retina that involves the rods of the eyes. A reduced sharpness of vision and night blindness are usually the only symptoms. The non-progressive disorder is linked to a defect at chromosome Xp11.23 and occurs only in males though females may be carriers.

Night blindness, congenital stationary, type 2A: Introduction

Types of Night blindness, congenital stationary, type 2A:

Broader types of Night blindness, congenital stationary, type 2A:

What causes Night blindness, congenital stationary, type 2A?

Causes of Night blindness, congenital stationary, type 2A: see causes of Night blindness, congenital stationary, type 2A

What are the symptoms of Night blindness, congenital stationary, type 2A?

Symptoms of Night blindness, congenital stationary, type 2A: see symptoms of Night blindness, congenital stationary, type 2A

Night blindness, congenital stationary, type 2A: Testing

Diagnostic testing: see tests for Night blindness, congenital stationary, type 2A.

Misdiagnosis: see misdiagnosis and Night blindness, congenital stationary, type 2A.

How is it treated?

Doctors and Medical Specialists for Night blindness, congenital stationary, type 2A: Medical Geneticist, Ophthalmologist ; see also doctors and medical specialists for Night blindness, congenital stationary, type 2A.
Treatments for Night blindness, congenital stationary, type 2A: see treatments for Night blindness, congenital stationary, type 2A

Name and Aliases of Night blindness, congenital stationary, type 2A

Main name of condition: Night blindness, congenital stationary, type 2A

Other names or spellings for Night blindness, congenital stationary, type 2A:

CSNB2A, CSNB, incomplete, X-linked

 

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